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GGATTCCTGGGGTGCTGGTGTGTGT[C/T]CTTTCAGGAGGTGGTAACATTTGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608216 MIM: 194531 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
COMMD5 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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COMMD5 - COMM domain containing 5 | ||||||
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There are no transcripts associated with this gene. |
ZNF7 - zinc finger protein 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282795.1 | 124 | Missense Mutation | TCC,TTC | S,F 10 | NP_001269724.1 | |
NM_001282796.1 | 124 | Intron | NP_001269725.1 | |||
NM_001282797.1 | 124 | Intron | NP_001269726.1 | |||
NM_003416.3 | 124 | Intron | NP_003407.1 | |||
XM_006716654.2 | 124 | Intron | XP_006716717.1 | |||
XM_006716656.3 | 124 | Intron | XP_006716719.1 | |||
XM_011517291.2 | 124 | Missense Mutation | TCC,TTC | S,F 16 | XP_011515593.1 | |
XM_011517292.2 | 124 | Missense Mutation | TCC,TTC | S,F 10 | XP_011515594.1 | |
XM_011517293.2 | 124 | Intron | XP_011515595.1 | |||
XM_011517294.2 | 124 | Intron | XP_011515596.1 | |||
XM_011517295.2 | 124 | Intron | XP_011515597.1 | |||
XM_011517296.2 | 124 | Intron | XP_011515598.1 | |||
XM_011517297.2 | 124 | Intron | XP_011515599.1 | |||
XM_017013813.1 | 124 | Missense Mutation | TCC,TTC | S,F 16 | XP_016869302.1 | |
XM_017013814.1 | 124 | Missense Mutation | TCC,TTC | S,F 20 | XP_016869303.1 | |
XM_017013815.1 | 124 | Missense Mutation | TCC,TTC | S,F 20 | XP_016869304.1 | |
XM_017013816.1 | 124 | Missense Mutation | TCC,TTC | S,F 16 | XP_016869305.1 | |
XM_017013817.1 | 124 | Missense Mutation | TCC,TTC | S,F 10 | XP_016869306.1 |